Linked Data
dbSNP Id:
rs1057523975
gnomAD v4:
10-87965421-A-T
MyVariant Identifiers:
chr10:g.89725178A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87965421A>T , CM000672.2:g.87965421A>T | GRCh38 |
| NC_000010.10:g.89725178A>T , CM000672.1:g.89725178A>T | GRCh37 |
| NC_000010.9:g.89715158A>T | NCBI36 |
| NG_007466.2:g.106983A>T , LRG_311:g.106983A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700029.2:c.1254A>T | ENSP00000514759.2:p.Pro418= | |
| ENST00000710265.1:c.*190A>T | ENSP00000518161.1:n.*190A>T | |
| ENST00000688158.2:n.1896A>T | ||
| ENST00000688922.2:c.*991A>T | ENSP00000508742.2:n.*991A>T | |
| ENST00000700021.1:c.1116A>T | ENSP00000514757.1:p.Pro372= | |
| ENST00000700022.1:c.*500A>T | ENSP00000514758.1:n.*500A>T | |
| ENST00000700023.1:n.2319A>T | ||
| ENST00000700024.1:n.2553A>T | ||
| ENST00000706954.1:c.1161A>T | ENSP00000516674.1:p.Pro387= | |
| ENST00000706955.1:c.*1196A>T | ENSP00000516675.1:n.*1196A>T | |
| ENST00000686459.1:c.*747A>T | ENSP00000508909.1:n.*747A>T | |
| ENST00000688158.1:c.*1272A>T | ENSP00000509254.1:n.*1272A>T | |
| ENST00000688308.1:c.1161A>T | ENSP00000508752.1:p.Pro387= | |
| ENST00000688922.1:c.1082A>T | ||
| ENST00000693560.1:c.1680A>T | ENSP00000509861.1:p.Pro560= | |
| ENST00000371953.8:c.1161A>T MANE Select | ENSP00000361021.3:p.Pro387= | |
| ENST00000371953.7:c.1161A>T | ENSP00000361021.3:p.Pro387= | |
| NM_000314.5:c.1161A>T | NP_000305.3:p.Pro387= | |
| NM_000314.6:c.1161A>T | NP_000305.3:p.Pro387= | |
| NM_001304717.2:c.1680A>T | NP_001291646.2:p.Pro560= | |
| NM_001304718.1:c.570A>T | NP_001291647.1:p.Pro190= | |
| XM_006717926.2:c.1116A>T | XP_006717989.1:p.Pro372= | |
| XM_011539982.1:c.1065A>T | XP_011538284.1:p.Pro355= | |
| XR_945791.1:n.1731A>T | ||
| NM_000314.7:c.1161A>T | NP_000305.3:p.Pro387= | |
| NM_001304717.5:c.1680A>T | NP_001291646.4:p.Pro560= | |
| NM_001304718.2:c.570A>T | NP_001291647.1:p.Pro190= | |
| NM_000314.8:c.1161A>T MANE Select | NP_000305.3:p.Pro387= |